Impact of Positron Emission Tomography (PET) Imaging in Women With Locally Advanced Cervical Cancer (PET LACE Trial)

NCT00895349 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 171

Last updated 2020-01-29

No results posted yet for this study

Summary

The purpose of this trial is to improve the clinical management and outcome of patients with locally advanced cervical cancer by using positron emission tomography-computed tomography (PET-CT) imaging.

There is considerable debate worldwide regarding the utility of PET for staging cervical cancer. Although there are studies on the accuracy (sensitivity and specificity) of PET in cervical cancer, there are currently no prospective randomized studies on how PET information affects treatment decisions and outcomes.

Conditions

Interventions

PROCEDURE

CT Abdomen and Pelvis scan + whole body PET-CT scan

Pre-treatment scan

PROCEDURE

CT Abdomen and Pelvis scan

Pre-treatment scan

Sponsors & Collaborators

  • Ontario Ministry of Health and Long Term Care

    collaborator OTHER_GOV
  • Ontario Clinical Oncology Group (OCOG)

    lead OTHER

Principal Investigators

  • Laurie Elit, MD · Juravinski Cancer Centre, Canada

  • Anthony Fyles, MD · Princess Margaret Hospital, Canada

  • Greg Pond, PhD · Ontario Clinical Oncology Group/McMaster University, Department of Oncology

  • Mark Levine, MD · Ontario Clinical Oncology Group/McMaster University, Department of Oncology

  • Karen Gulenchyn, MD · Hamilton Health Sciences Centre

  • Mostafa Atri, MD · University Health Network, Toronto

  • Douglas Coyle, PhD · University of Ottawa Epidemiology & Community Medicine

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-04-30
Primary Completion
2014-06-30
Completion
2019-08-31

Countries

  • Canada

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00895349 on ClinicalTrials.gov